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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 412962Generated: October 29, 2026

Ammonium Chloride → HCID 18537395, compound

https://huagongshe.com/reaction/412962

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
ReactantTrimethylaluminumHCID 16682925—
ReactantHCID 18536857HCID 18536857—
ReactantHCID 18537416HCID 18537416—
SolventTolueneHCID 1140—
SolventDimethylformamideHCID 6228—
SolventDichloromethane methanolHCID 21226129—
ProductHCID 18537395HCID 1853739544%

Reaction Steps

4-[4-(3-Hydroxy-4-methoxyphenyl)(1,3-thiazol-2-yl)]-5-methylthiothiophene-2-carboxamidine hydrochiloride: A portion of the mixture (320 mg, ca. 0.788 mmol as based on the 1H-NMR spectrum) containing the 2-methoxy-5-{2-[5-(methoxvcarbonyl)-2-methylthio(3-thienyl)](1,3-thiazol-4-yl)}phenyl acetate (as prepared in the previous step) was treated according to the procedure in Example 10, step (b), using 415 mg (7.76 mmol) of ammonium chloride in 3.5 mL of toluene and 3.88 mL (7.66 mmol) of 2 M trimethylaluminum in toluene. After chromatography of the resulting residue on a 10 g silica SPE column (Waters Sep-Pak) with 10-40% MeOH-CH2Cl2, a light yellow solid was obtained which was dissolved in 45 mL of DMF and filtered to remove silica gel. Concentration under high vacuum and recrystallization from MeOH—Et2O afforded the title compound as a light tan solid (132 mg, 44%). 1H-NMR (300 MHz, DMSO-d6) δ 9.49 (broad s, 2H), 9.16 (broad s, 2H), 8.67 (s, 1H), 7.98 (s, 1H), 7.5 (obscured m, 3H), 7.00 (obscured d, 1H, J=8.3 Hz), 3.82 (s, 3H), and 2.79 (s, 3H). Mass spectrum (ESI) calcd. for C16H15N3O2S3: 378.0 (M+H). Found: 378.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06562840B1
Source datasetuspto-grants-2003_05
ORD IDord-b225de112ae34addab584105b1e950a5
Source noteuspto-grants-2003_05